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Equaline all day allergy - 41163-458-76 - (Cetirizine Hydrochloride)

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Drug Information of Equaline all day allergy

Product NDC: 41163-458
Proprietary Name: Equaline all day allergy
Non Proprietary Name: Cetirizine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Cetirizine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Equaline all day allergy

Product NDC: 41163-458
Labeler Name: Supervalu Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078336
Marketing Category: ANDA
Start Marketing Date: 20080123

Package Information of Equaline all day allergy

Package NDC: 41163-458-76
Package Description: 1 BOTTLE in 1 CARTON (41163-458-76) > 120 TABLET in 1 BOTTLE

NDC Information of Equaline all day allergy

NDC Code 41163-458-76
Proprietary Name Equaline all day allergy
Package Description 1 BOTTLE in 1 CARTON (41163-458-76) > 120 TABLET in 1 BOTTLE
Product NDC 41163-458
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080123
Marketing Category Name ANDA
Labeler Name Supervalu Inc
Substance Name CETIRIZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Equaline all day allergy


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